A flexible, hand-held manual surgical instrument designed to be introduced through the working channel of an endoscope to grasp tissue (typically atraumatically), or additionally foreign bodies. It has proximal controls (e.g., scissors-like handles), a flexibl
| Company | Devices | Share |
|---|---|---|
| Surgical Direct, Inc. | 1,044 | 77% |
| Hangzhou Ags Medtech Co., Ltd. | 107 | 8% |
| Zhejiang Chuangxiang Medical Technology Co., Ltd. | 54 | 4% |
| Cook Incorporated | 34 | 3% |
| Yangzhou Fartley Medical Instrument Technology Co., Ltd | 11 | 1% |
| Ovesco Endoscopy Ag | 10 | 1% |
| Modern Surgical Instruments Llc | 10 | 1% |
| Alton (Shanghai) Medical Instruments Co., Ltd. | 9 | 1% |
| Anrei Medical(Hz) Co.,Ltd. | 9 | 1% |
| Lagis Enterprise Co., Ltd. | 9 | 1% |
| Olympus Medical Systems Corp. | 8 | 1% |
| Micro-Tech (Nanjing) Co., Ltd. | 7 | 1% |
Company = labeler of record on GUDID. 34 companies in total; top 12 shown. Click headers to sort.
Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.
| Code | Name | Devices |
|---|---|---|
| GCJ | Laparoscope, general & plastic surgery | 973 |
| PTS | Endoscopic Grasping/Cutting Instrument, Non-Powered, Exempt | 156 |
| GCJ | Laparoscope, General & Plastic Surgery | 77 |
| OCZ | Endoscopic Grasping/Cutting Instrument, Non-Powered | 76 |
| FFL | DISLODGER, STONE, BASKET, URETERAL, METAL | 22 |
| GEI | Electrosurgical, Cutting & Coagulation & Accessories | 10 |
Use these as the dimensions to specify in a tender line.
1,358 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Flexible endoscopic tissue manipulation forceps, single-use", from 34 companies. The largest labeler is Surgical Direct, Inc. with 77% of records.
GCJ (Laparoscope, general & plastic surgery), PTS (Endoscopic Grasping/Cutting Instrument, Non-Powered, Exempt), GCJ (Laparoscope, General & Plastic Surgery), OCZ (Endoscopic Grasping/Cutting Instrument, Non-Powered)
No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.
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Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.